OSC0033 AND nstd224 - dbVar - NCBI

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Items: 9

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Number of Variants: 9

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6630933	copy number variation	1	nstd224	human		GRCh37 chr6: 128,691,353-128,745,590 , GRCh38.p12 chr6: 128,370,208-128,424,445 , GRCh38.p12 chr6\|NT_187556.1: 719,542-773,779	PTPRK
nsv6628914	copy number variation	179	nstd224	human		GRCh37 chr3: 173,259,356-173,289,281 , GRCh38.p12 chr3: 173,541,566-173,571,491	NLGN1
nsv6624765	copy number variation	10	nstd224	human		GRCh37 chr19: 43,654,209-43,708,179 , GRCh38.p12 chr19: 43,150,057-43,204,027	PSG5, PSG4, 1 more genes
nsv6621730	copy number variation	83	nstd224	human		GRCh37 chr12: 63,946,056-64,116,159 , GRCh38.p12 chr12: 63,552,276-63,722,379	LOC100418730, S100A11P4, 1 more genes
nsv6623511	copy number variation	61	nstd224	human		GRCh37 chr16: 75,539,436-75,577,559 , GRCh38.p12 chr16: 75,505,538-75,543,661	CHST5, TMEM231, 1 more genes
nsv6621645	copy number variation	1	nstd224	human		GRCh37 chr13: 110,236,646-115,091,330 , GRCh38.p12 chr13: 109,584,299-114,325,855	PARP1P1, F7, 103 more genes
nsv6625837	copy number variation	1	nstd224	human		GRCh37 chr1: 148,529,087-149,161,732 , GRCh38.p12 chr1: 143,398,568-144,488,566	RNVU1-18, RPL22P5, 49 more genes
nsv6628233	copy number variation	60	nstd224	human		GRCh37 chr2: 89,442,329-90,229,318 , GRCh38.p12 chr2: 89,142,846-90,190,466	IGKV6D-21, IGKV3D-25, 59 more genes
nsv6622438	copy number variation	1	nstd224	human		GRCh37 chr14: 105,773,028-107,287,663 , GRCh38.p12 chr14: 105,306,691-106,879,456 , GRCh38.p12 chr14\|NT_187600.1: 1-1,214,078	CRIP2, BRF1, 214 more genes

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OSC0033 AND nstd224 (10)
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